Variant report

Variant rs4741460
Chromosome Location chr9:15100861-15100862
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:15099200-15101200 Enhancers HepG2 liver
2 chr9:15100000-15101000 Enhancers Fetal Kidney kidney
3 chr9:15100000-15101200 Flanking Active TSS Fetal Lung lung
4 chr9:15100000-15101600 Enhancers Fetal Heart heart
5 chr9:15100000-15101600 Enhancers Fetal Muscle Leg muscle
6 chr9:15100000-15101800 Enhancers Fetal Stomach stomach
7 chr9:15100400-15101400 Weak transcription Placenta Placenta
8 chr9:15100800-15101400 Enhancers Fetal Brain Female brain
9 chr9:15100800-15101600 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr9:15100800-15102000 Active TSS Fetal Brain Male brain

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